Wakita T, Kakumu S, Shibata M, Yoshioka K, Ito Y, Shinagawa T, Ishikawa T, Takayanagi M, Morishima T
Third Department of Internal Medicine, Nagoya University School of Medicine, Japan.
J Clin Invest. 1991 Dec;88(6):1793-801. doi: 10.1172/JCI115500.
We analyzed the pre-C and core region of hepatitis B virus (HBV) DNA by a polymerase chain reaction in 22 chronic carriers. In 9 hepatitis B e antigen-positive asymptomatic carriers, a single DNA band was detected at the expected size, whereas additional shorter DNA bands were observed in 7 out of 11 patients with chronic hepatitis. The smaller-sized DNAs from one chronic hepatitis patient had various lengths of deletions spanning from 105 to 183 bp in the middle of the core gene, and all deletions included common nucleotide sequences. All of the smaller-sized DNAs from the other patients proved to be variant core genes. They were deleted in similar regions by Southern analysis using oligonucleotide probes. A follow-up study revealed that four out of seven chronic hepatitis patients with a short core gene seroconverted to antibody to hepatitis B e antigen, but those with only a "wild type" did not. In another set of sequence studies, clones isolated from two chronic carriers displayed heterogeneity of the pre-C and core gene which was more often present in sera with normal alanine aminotransferase levels than with abnormal levels. These results suggest that mutant HBV alters the host immune response, and may modulate the clinical course of HBV infection. An alternative possibility is that chronic hepatitis selects for mutant forms.
我们采用聚合酶链反应对22例慢性携带者的乙肝病毒(HBV)DNA的前C区和核心区进行了分析。在9例乙肝e抗原阳性的无症状携带者中,在预期大小处检测到一条单一的DNA条带,而在11例慢性肝炎患者中的7例中观察到了额外的较短DNA条带。一名慢性肝炎患者的较小尺寸DNA在核心基因中间有105至183 bp的各种长度的缺失,所有缺失都包含共同的核苷酸序列。其他患者的所有较小尺寸DNA均被证明是变异的核心基因。使用寡核苷酸探针通过Southern分析发现它们在相似区域缺失。一项随访研究显示,7例核心基因短的慢性肝炎患者中有4例血清转化为乙肝e抗原抗体,而只有“野生型”基因的患者则没有。在另一组序列研究中,从两名慢性携带者中分离出的克隆显示前C区和核心基因存在异质性,在丙氨酸转氨酶水平正常的血清中比在异常水平的血清中更常见。这些结果表明,突变的HBV改变了宿主免疫反应,并可能调节HBV感染的临床进程。另一种可能性是慢性肝炎选择了突变形式。